A curated catalogue of human genomic structural variation




Variant Details

Variant: nssv17436362



Internal ID22494232
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr9:8323730..8326709hg38UCSC Ensembl
chr9:8323730..8326709hg19UCSC Ensembl
Cytoband9p24.1
Allele length
AssemblyAllele length
hg382980
hg192980
Variant TypeOTHER inversion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsnsv5971317
Supporting Variants
Samples
Known GenesPTPRD
MethodSequencing
Analysis
Platform
CommentsDESC=[BREAKPOINT1]
ReferenceAlmarri_et_al_2020
Pubmed ID32531199
Accession Number(s)nssv17436362
Frequency
Sample Size914
Observed Gain0
Observed Loss0
Observed Complex0
Frequencyn/a


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